Nothing Special   »   [go: up one dir, main page]

AU2001273574A1 - Substituted 5-alkynyl pyrimidines having neurotrophic activity - Google Patents

Substituted 5-alkynyl pyrimidines having neurotrophic activity

Info

Publication number
AU2001273574A1
AU2001273574A1 AU2001273574A AU7357401A AU2001273574A1 AU 2001273574 A1 AU2001273574 A1 AU 2001273574A1 AU 2001273574 A AU2001273574 A AU 2001273574A AU 7357401 A AU7357401 A AU 7357401A AU 2001273574 A1 AU2001273574 A1 AU 2001273574A1
Authority
AU
Australia
Prior art keywords
substituted
neurotrophic activity
pyrimidines
alkynyl
disorders
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
AU2001273574A
Inventor
Lilia Beauchamp
James L. Kelley
Thomas A. Krenitsky
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Krenitsky Pharmaceuticals Inc
Original Assignee
Krenitsky Pharmaceuticals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Krenitsky Pharmaceuticals Inc filed Critical Krenitsky Pharmaceuticals Inc
Publication of AU2001273574A1 publication Critical patent/AU2001273574A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6509Six-membered rings
    • C07F9/6512Six-membered rings having the nitrogen atoms in positions 1 and 3

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Diabetes (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Psychiatry (AREA)
  • Hematology (AREA)
  • Hospice & Palliative Care (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

The present invention relates to a series of novel substituted 5-alkynyl pyrimidines, pharmaceutical compositions which contain them, methods for their preparation, and their use in therapy, particularly in the treatment of neurodegenerative or other neurological disorders of the central and peripheral nervous systems, including age related cognitive disorders such as senility and Alzheimer's disease, nerve injuries, peripheral neuropathies, and seizure disorders such as epilepsy.
AU2001273574A 2000-07-24 2001-07-20 Substituted 5-alkynyl pyrimidines having neurotrophic activity Abandoned AU2001273574A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22034800P 2000-07-24 2000-07-24
US60220348 2000-07-24
PCT/US2001/023088 WO2002008205A1 (en) 2000-07-24 2001-07-20 Substituted 5-alkynyl pyrimidines having neurotrophic activity

Publications (1)

Publication Number Publication Date
AU2001273574A1 true AU2001273574A1 (en) 2002-02-05

Family

ID=22823191

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2001273574A Abandoned AU2001273574A1 (en) 2000-07-24 2001-07-20 Substituted 5-alkynyl pyrimidines having neurotrophic activity

Country Status (10)

Country Link
US (1) US7205297B2 (en)
EP (1) EP1303495B1 (en)
JP (2) JP5154728B2 (en)
AT (1) ATE469132T1 (en)
AU (1) AU2001273574A1 (en)
CA (1) CA2416442C (en)
DE (1) DE60142236D1 (en)
DK (1) DK1303495T3 (en)
ES (1) ES2346513T3 (en)
WO (1) WO2002008205A1 (en)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7378526B2 (en) * 2002-05-07 2008-05-27 Neurosearch A/S Azacyclic ethynyl derivatives
UA80888C2 (en) * 2003-06-05 2007-11-12 Hoffmann La Roche Imidazole derivatives as glutmate receptor antagonists
US7531529B2 (en) 2003-06-05 2009-05-12 Roche Palo Alto Llc Imidazole derivatives
CN100462363C (en) 2003-06-12 2009-02-18 弗·哈夫曼-拉罗切有限公司 Heteroaryl-substituted imdazole derivatives as glutamate receptor antagonists
WO2005016914A1 (en) * 2003-08-14 2005-02-24 Smithkline Beecham Corporation Chemical compounds
ATE402705T1 (en) * 2003-12-24 2008-08-15 Astrazeneca Ab PYRIMIDINES WITH TIE2 (TEK) ACTIVITY
ATE415970T1 (en) * 2003-12-24 2008-12-15 Astrazeneca Ab PYRIMIDINES WITH TIE2 (TEK) ACTIVITY
PT1756086E (en) 2004-06-01 2008-08-08 Hoffmann La Roche Pyridin-4-yl-ethynyl-imidazoles and pyrazoles as mglu5 receptor antagonists
US7776869B2 (en) 2004-10-18 2010-08-17 Amgen Inc. Heteroaryl-substituted alkyne compounds and method of use
AU2005306458B2 (en) * 2004-11-17 2011-02-17 Miikana Therapeutics, Inc. Kinase inhibitors
EP1863805A1 (en) * 2005-02-01 2007-12-12 AstraZeneca AB Pyrimidine compounds having tie2 (tek) inhibitory activity
JP4993205B2 (en) * 2005-03-30 2012-08-08 塩野義製薬株式会社 Pyrimidine derivatives having tyrosine kinase inhibitory action
JP5597353B2 (en) * 2005-09-30 2014-10-01 ミイカナ セラピューティクス インコーポレイテッド Substituted pyrazole compounds
ES2699585T3 (en) 2006-12-15 2019-02-11 Nantbio Inc Triazine derivatives and their therapeutic applications
ES2577391T3 (en) 2006-12-21 2016-07-14 F. Hoffmann-La Roche Ag Polymorphs of an mglur5 receptor antagonist
JP2010529193A (en) * 2007-06-11 2010-08-26 ミイカナ セラピューティクス インコーポレイテッド Substituted pyrazole compounds
US10131904B2 (en) * 2008-02-11 2018-11-20 Rxi Pharmaceuticals Corporation Modified RNAi polynucleotides and uses thereof
WO2010008582A2 (en) 2008-07-18 2010-01-21 Rxi Pharmaceuticals Corporation Phagocytic cell drug delivery system
AR072845A1 (en) * 2008-07-29 2010-09-22 Boehringer Ingelheim Int 5-ALQUIL-PIRIMIDINAS AND ITS USE IN THE TREATMENT OF DISEASES MEDIATED BY THE ACTIVITY OF KINASES.
US8541434B2 (en) 2008-08-20 2013-09-24 Merck Sharp & Dohme Corp. Ethynyl-substituted pyridine and pyrimidine derivatives and their use in treating viral infections
ES2439009T3 (en) 2008-08-20 2014-01-21 Merck Sharp & Dohme Corp. Pyridine and pyrimidine derivatives substituted with ethenyl and their use in the treatment of viral infections
EP2326627A1 (en) 2008-08-20 2011-06-01 Schering Corporation Substituted pyridine and pyrimidine derivatives and their use in treating viral infections
EP2326628A1 (en) 2008-08-20 2011-06-01 Schering Corporation Azo-substituted pyridine and pyrimidine derivatives and their use in treating viral infections
WO2010033247A2 (en) 2008-09-22 2010-03-25 Rxi Pharmaceuticals Corporation Reduced size self-delivering rnai compounds
US9074211B2 (en) 2008-11-19 2015-07-07 Rxi Pharmaceuticals Corporation Inhibition of MAP4K4 through RNAI
WO2010078536A1 (en) 2009-01-05 2010-07-08 Rxi Pharmaceuticals Corporation Inhibition of pcsk9 through rnai
WO2010090762A1 (en) 2009-02-04 2010-08-12 Rxi Pharmaceuticals Corporation Rna duplexes with single stranded phosphorothioate nucleotide regions for additional functionality
US9078902B2 (en) 2009-06-09 2015-07-14 Nantbioscience, Inc. Triazine derivatives and their therapeutical applications
EP2440053A4 (en) 2009-06-09 2012-10-31 California Capital Equity Llc Benzyl substituted triazine derivatives and their therapeutical applications
CA2778979C (en) * 2009-10-30 2018-04-24 Janssen Pharmaceutica Nv Phenoxy-substituted pyrimidines as opioid receptor modulators
UY33199A (en) * 2010-01-26 2011-08-31 Boehringer Ingelheim Int 5-ALQUINIL-PYRIMIDINS.
UY33198A (en) * 2010-01-26 2011-08-31 Boehringer Ingelheim Int 5-ALQUINIL-PYRIMIDINS.
EP2550002B1 (en) 2010-03-24 2019-05-08 Phio Pharmaceuticals Corp. Rna interference in dermal and fibrotic indications
WO2011119871A1 (en) 2010-03-24 2011-09-29 Rxi Phrmaceuticals Corporation Rna interference in ocular indications
RU2615143C2 (en) 2010-03-24 2017-04-04 Адвирна Self-delivered rnai compounds of reduced size
UA110995C2 (en) * 2011-10-07 2016-03-10 Ф. Хоффманн-Ля Рош Аг ETHINYL DERIVATIVES AS MODULATORS OF THE METABOTROPIC GLUTAMATE RECEPTOR
US10934550B2 (en) 2013-12-02 2021-03-02 Phio Pharmaceuticals Corp. Immunotherapy of cancer
EP3077050B1 (en) 2013-12-04 2020-10-21 Phio Pharmaceuticals Corp. Methods for treatment of wound healing utilizing chemically modified oligonucleotides
WO2015168108A2 (en) 2014-04-28 2015-11-05 Rxi Pharmaceuticals Corporation Methods for treating cancer using nucleic targeting mdm2 or mycn
JP2017514908A (en) 2014-05-01 2017-06-08 アールエックスアイ ファーマシューティカルズ コーポレーション Methods for the treatment of disorders in the front of the eye utilizing nucleic acid molecules
CN107073294A (en) 2014-09-05 2017-08-18 阿克赛医药公司 Use the method for targeting TYR or MMP1 exonuclease treatment aging and skin disorder
WO2017007825A1 (en) 2015-07-06 2017-01-12 Rxi Pharmaceuticals Corporation Methods for treating neurological disorders using a synergistic small molecule and nucleic acids therapeutic approach
US11001845B2 (en) 2015-07-06 2021-05-11 Phio Pharmaceuticals Corp. Nucleic acid molecules targeting superoxide dismutase 1 (SOD1)
JP2018531037A (en) 2015-10-19 2018-10-25 アールエックスアイ ファーマシューティカルズ コーポレーション Reduced size self-delivering nucleic acid compounds targeting long non-coding RNAs
JP2023501445A (en) 2019-11-08 2023-01-18 フィオ ファーマシューティカルズ コーポレーション Chemically modified oligonucleotides targeting bromodomain-containing protein 4 (BRD4) for immunotherapy
US20230089478A1 (en) 2019-12-31 2023-03-23 Phio Pharmaceuticals Corp. Chemically modified oligonucleotides with improved systemic delivery
JP2024529025A (en) 2021-08-04 2024-08-01 フィオ ファーマシューティカルズ コーポレーション Chemically Modified Oligonucleotides
WO2023015264A1 (en) 2021-08-04 2023-02-09 Phio Pharmaceuticals Corp. Immunotherapy of cancer utilizing natural killer cells treated with chemically modified oligonucleotides

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2691655A (en) * 1952-05-24 1954-10-12 Burroughs Wellcome Co 2-amino-4-substituted amino-6-aryl pyrimidines and process of preparing same
GB951432A (en) * 1959-03-17 1964-03-04 Wellcome Found Pyrimidine derivatives and the manufacture thereof
US3862190A (en) * 1972-09-08 1975-01-21 Pfizer 5-(unsubstituted and substituted phenoxy)-4-amino pyrimidines
DK397574A (en) * 1973-08-24 1975-04-28 Ciba Geigy Ag
GB1523274A (en) 1974-08-05 1978-08-31 Ici Ltd Herbicidal compositions containing substituted pyrimidine
FR2358148A1 (en) 1976-07-12 1978-02-10 Dick Pr 2,4-Di:amino pyrimidine sodium sulphonate cpds. - useful as water soluble antibacterials and sulphonamide potentiators
FR2397407A2 (en) 1977-07-11 1979-02-09 Dick Pierre 2,4-DIAMINO PYRIMIDINE DERIVATIVES AND THEIR SOLUTION IN ASSOCIATION WITH SULFAMIDS
US4508560A (en) * 1981-11-11 1985-04-02 Ciba Geigy Corporation Certain pyridylacetylene compounds, compositions containing same and herbicidal methods of use
US4663334A (en) * 1985-12-11 1987-05-05 Mcneilab, Inc. Heteroaromatic acetylenes useful as antihypertensive agents
FI895821A0 (en) 1988-12-07 1989-12-05 Wellcome Found PHARMACEUTICAL ACTIVE CNS FOERENINGAR.
GB9012316D0 (en) 1990-06-01 1990-07-18 Wellcome Found Pharmacologically active cns compounds
IE912114A1 (en) 1990-07-02 1992-01-15 Union Pharma Scient Appl Novel pyrimidine derivatives which are angiotensin ii¹receptor antagonists, their methods of preparation and¹pharmaceutical compositions in which they are present
US5075305A (en) * 1991-03-18 1991-12-24 Warner-Lambert Company Compound, composition and use
US5250532A (en) * 1991-04-11 1993-10-05 Dowelanco 3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides
DE69201559T2 (en) 1991-04-17 1995-07-13 Pfizer PYRIMIDINE DERIVATIVES FOR INCREASING ANTITUM ORACTIVITY.
US5336677A (en) 1991-10-24 1994-08-09 American Home Products Corporation Substituted aminopyrimidines as antihypertensives
GB9125842D0 (en) 1991-12-04 1992-02-05 Ici Plc Heterocyclic derivatives
WO1994014780A1 (en) 1992-12-18 1994-07-07 The Wellcome Foundation Limited Pyrimidine, pyridine, pteridinone and indazole derivatives as enzyme inhibitors
WO1994020508A1 (en) 1993-03-08 1994-09-15 Eisai Co., Ltd. Phosphonic acid derivatives
ES2114662T3 (en) 1993-08-26 1998-06-01 Ono Pharmaceutical Co DERIVATIVES OF 4-AMINOPYRIMIDINE.
JPH08283246A (en) 1994-06-01 1996-10-29 Nippon Soda Co Ltd Pyrimidine derivative, its production and controlling agent for pest
CA2217034A1 (en) 1995-04-03 1996-10-10 Sumitomo Pharmaceuticals Company, Limited Novel pyrimidine derivatives effective as psychotropic drug and process for the production thereof
TW544448B (en) * 1997-07-11 2003-08-01 Novartis Ag Pyridine derivatives
US6440965B1 (en) 1997-10-15 2002-08-27 Krenitsky Pharmaceuticals, Inc. Substituted pyrimidine derivatives, their preparation and their use in the treatment of neurodegenerative or neurological disorders of the central nervous system
US6583148B1 (en) * 1999-04-08 2003-06-24 Krenitsky Pharmaceuticals, Inc. Neurotrophic substituted pyrimidines

Also Published As

Publication number Publication date
EP1303495B1 (en) 2010-05-26
ATE469132T1 (en) 2010-06-15
ES2346513T3 (en) 2010-10-18
EP1303495A1 (en) 2003-04-23
WO2002008205A1 (en) 2002-01-31
JP2012229218A (en) 2012-11-22
CA2416442A1 (en) 2002-01-31
DK1303495T3 (en) 2010-09-20
JP5154728B2 (en) 2013-02-27
CA2416442C (en) 2010-06-08
US20040087789A1 (en) 2004-05-06
US7205297B2 (en) 2007-04-17
JP2004504386A (en) 2004-02-12
DE60142236D1 (en) 2010-07-08

Similar Documents

Publication Publication Date Title
AU2001273574A1 (en) Substituted 5-alkynyl pyrimidines having neurotrophic activity
AU4331400A (en) Neurotrophic substituted pyrimidines
AP2004003069A0 (en) 3-beta-d-ribofuranosynthiazolo [4-5-d] pyridimine nucleosides and uses thereof.
IL225192A (en) Combination of dextromethorphan and quinidine for use in the treatment of mental illness, neuropathic pain or brain injury
WO2001009118A3 (en) Dithiolthione compounds for the treatment of neurological disorders and for memory enhancement
AU2001236904A1 (en) Deep brain stimulation system for the treatment of parkinson's disease or other disorders
WO2003002596A3 (en) Use of dipeptidyl peptidase iv inhibitors as therapeutics for neurological disorders
WO2003092580A3 (en) Methods and compositions for treatment of central and peripheral nervous system disorders and novel compounds useful therefor
IL118836A0 (en) Pharmaceutical compositions comprising S-(-)N-propargyl-1-aminoindan
IL147271A0 (en) Compounds that bind her2
EA200200183A1 (en) COMPOSITION, CONTAINING TRAMADOL AND CONDITIONING DRUGS
TW200500344A (en) Novel compounds
MY120976A (en) 2-amino-6-(2-substituted-4-phenoxy)- substituted- pyridines
SG157231A1 (en) Substituted p-diaminobenzene derivatives
MY124786A (en) Bis-arylsulfones
DE69807587D1 (en) Quinazolin-4-one AMPA antagonists
EP1032556A4 (en) Pharmaceutically active compounds and methods of use
PT1463735E (en) Imidazo¬2,1-b -1,3,4-thiadiazole sulfonamides
EP1736470A3 (en) Pyrimidine derivatives as CB2 cannabinoid receptor modulators
TW200612969A (en) 3-β-d-ribofuranosylthiazolo[4,5-d]pyrimidine nucleosides and uses thereof
BR9803385A (en) Atropisomers of 2,3-disubstituted- (5,6) -heteroaryl condensate-pyrimidin-4-ones.
AP9901473A0 (en) Use of benzopyranols to treat neurological disorders.
IL143382A0 (en) Human adult astrocytes, their preparation and uses thereof
MX2007007472A (en) Triazolone, tetrazolone and imidazolone derivatives for use as alpha-2c adrenoreceptor antagonists.
IL136306A (en) Bis (fluorophenyl) alkylamides and related compounds, pharmaceutical compositions comprising them and their use in treating neurological disease or disorder